Isolation method for water insoluble components of a biomass and products provided therefrom

ABSTRACT

The process includes pretreating the biomass with a first basic solution such as sodium hydroxide and mechanically altering the fibers to provide a fluidized biomass. The fluidized biomass is then subjected to high frequency pulses and shear forces without denaturing the individual components of the biomass. The biomass is then subjected to compressive force to separate a first liquid fraction from a first fractionated biomass. The first fractionated biomass may again then be subjected to the same high frequency pulses and shear forces as previously, particularly if there are hemicellulose and/or sugars still present in the first fractionated biomass. Compressive forces are used to separate a second liquid fraction from a second fractionated biomass. The second fractionated biomass is subjected to oxidation such as with hydrogen peroxide at a pH of 8 to 12. The second fractioned biomass is then subjected to compressive forces to separate one or more water insoluble components of the biomass in water soluble form.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims priority to U.S. Provisional Patent ApplicationSer. No. 61/864,853, filed Aug. 12, 2013, U.S. Provisional PatentApplication Ser. No. 61/909,418, filed Nov. 27, 2013, and U.S.Provisional Patent Application Ser. No. 61/919,194, filed Dec. 20, 2013,the disclosures of which are incorporated herein by reference in theirentirety.

FIELD OF THE INVENTION

The present invention relates to a process for isolating components of abiomass. Examples of fractions and extractives provided in the processinclude the extraction, isolation, and purification of lignin,cellulose, sugars, hemicellulose, fibers and/or extractives.

BACKGROUND OF THE INVENTION

Natural cellulosic feedstocks are typically referred to as “biomass.”Many types of biomass, including wood, paper, agricultural residues,herbaceous crops, and lignocellulosic municipal and industrial solidwastes have been considered as feedstocks for the production andpreparation of a wide range of goods. Plant biomass materials arecomprised primarily of cellulose, hemicellulose and lignin, boundtogether in a complex and entangled gel-like structure along withamounts of extractables, pectins, proteins and/or ash. Thus, successfulcommercial use of biomass as a chemical feedstock depends on theefficient and/or economical separation and isolation of these variousconstituents.

Many steps are often required in production, harvesting, storage,transporting, and processing of biomass to yield useful products. Onestep in the processing is the separation, or fractionation, of thebiomass into its major components: extractives, hemicellulose, lignin,and cellulose. Many approaches have been investigated for disentanglingthe complex structure of the biomass. Once this separation has beenachieved, a variety of paths are opened for further processing of eachcomponent into marketable products. For example, the possibility ofproducing products such as biofuels, polymers and latex replacementsfrom biomass has recently received much attention. This attention is dueto the availability of large amounts of cellulosic feedstock, the needto minimize burning or landfilling of waste cellulosic materials, andthe usefulness of sugar and cellulose as raw materials substituting foroil-based products.

One component of the biomass that the isolation of which has been ofinterest is lignin. Lignin is a cross-linked racemic macromolecule withmolecular masses in excess of 10,000 Da. It is relatively hydrophobicand aromatic in nature. The degree of polymerization in nature isdifficult to measure, since it is often fragmented during typicalextraction and the molecule consists of various types of substructuresthat appear to repeat in a haphazard manner. Different types of ligninhave been described depending on the means of isolation. There are threemonolignol monomers, methoxylated to various degrees: p-coumarylalcohol, coniferyl alcohol, and sinapyl alcohol. These lignols areincorporated into lignin in the form of the phenylpropanoidsp-hydroxyphenyl (H), guaiacyl (G), and syringyl (S), respectively.Gymnosperms have a lignin that consists almost entirely of G with smallquantities of H. That of dicotyledonous angiosperms is more often thannot a mixture of G and S (with very little H), and monocotyledonouslignin is a mixture of all three. Many grasses have mostly G, while somepalms have mainly S. All lignins contain small amounts of incomplete ormodified monolignols, and other monomers are prominent in non-woodyplants.

Likewise, cellulose, another component of the biomass has also been ofparticular interest, particularly with respect to the paper industry andin the production of biofuels. Cellulose is an organic compound with theformula (C₆H₁₀O₅)_(n), a polysaccharide consisting of a linear chain ofseveral hundred to over ten thousand β(1→4) linked D-glucose units.Cellulose is an important structural component of the primary cell wallof green plants, many forms of algae and the oomycetes. Cellulose is anextremely abundant organic polymer on Earth. The cellulose content ofcotton fiber is 90%, that of wood is 40-50% and that of dried hemp isapproximately 45%. Cellulose is mainly used to produce paperboard andpaper. Smaller quantities are converted into a wide variety ofderivative products such as cellophane and rayon.

Thus, there continues to be a need for improved systems and methods forseparating solid biomass into its individual constituent components,particularly lignin, hemicelluloses, and cellulose that take intoconsideration factors such as environmental and energy concerns,efficiency and cost-effectiveness.

SUMMARY OF THE INVENTION

It should be appreciated that this Summary is provided to introduce aselection of concepts in a simplified form, the concepts being furtherdescribed below in the Detailed Description. This Summary is notintended to identify key features or essential features of thisdisclosure, nor is it intended to limit the scope of the invention.

The present invention provides a process for isolating variouscomponents of biomass that may be adapted to large-scale production,uses environmentally friendly solvents and/or is energy efficient.Moreover, the present invention provides a process for isolating variouswater insoluble components of the biomass in water soluble form whileproviding a biomass substantially devoid of hemicellulose, other sugars,and the water insoluble components.

The process includes pretreating the biomass with a first basic solutionsuch as sodium hydroxide. Pretreatment may include mechanically alteringthe fibers to, for example, open up the fibers and to form a fluidizedbiomass. The biomass with opened up fibers is then subjected to highfrequency pulses and shear forces without denaturing the individualcomponents of the biomass. The biomass is then subjected to compressiveforce to separate a first liquid fraction from a first fractionatedbiomass. The first fractionated biomass may again then be subjected tothe same high frequency pulses and shear forces as previously,particularly if there are hemicellulose and/or sugars still present inthe first fractionated biomass. Compressive forces are used to separatea second liquid fraction from a second fractionated biomass. The secondfractionated biomass is high in cellulose and water insoluble componentsincluding lignins and proteins, and is substantially devoid ofhemicelluloses and sugars. The second fractionated biomass is subjectedto oxidation such as with hydrogen peroxide at a pH of 8 to 12. Thesecond fractioned biomass is then subjected to compressive forces toseparate one or more water insoluble components of the biomass in watersoluble and liquid form from a second fractionated biomass substantiallydevoid of hemicellulose, sugar and the water insoluble components of thebiomass.

The present invention also provides a water insoluble component of abiomass in water soluble form at a pH of 5 to 12 at ambient temperature.Exemplary components which are typically water soluble includehemicellulose, sugars, pectins, some proteins and extractives.Components which are typically water insoluble include lipids, lignins,some proteins and extractives.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 depicts a flow chart that outlines an embodiment of the processof the invention.

FIG. 2 depicts a flow chart that outlines another embodiment of theprocess of the invention.

DETAILED DESCRIPTION OF EMBODIMENTS

In the following detailed description, embodiments of the presentinvention are described in detail to enable practice of the invention.Although the invention is described with reference to these specificembodiments, it should be appreciated that the invention can be embodiedin different forms and should not be construed as limited to theembodiments set forth herein. Rather, these embodiments are provided sothat this disclosure will be thorough and complete, and will fullyconvey the scope of the invention to those skilled in the art.

The terminology used in the description of the invention herein is forthe purpose of describing particular embodiments only and is notintended to be limiting of the invention. As used in the description ofthe invention and the appended claims, the singular forms “a,” “an” and“the” are intended to include the plural forms as well, unless thecontext clearly indicates otherwise. The invention includes numerousalternatives, modifications, and equivalents as will become apparentfrom consideration of the following detailed description.

It will be understood that although the terms “first,” “second,”“third,” “a),” “b),” and “c),” etc. may be used herein to describevarious elements of the invention should not be limited by these terms.These terms are only used to distinguish one element of the inventionfrom another. Thus, a first element discussed below could be termed aelement aspect, and similarly, a third without departing from theteachings of the present invention. Thus, the terms “first,” “second,”“third,” “a),” “b),” and “c),” etc. are not intended to necessarilyconvey a sequence or other hierarchy to the associated elements but areused for identification purposes only. The sequence of operations (orsteps) is not limited to the order presented in the claims or figuresunless specifically indicated otherwise. Steps may be conductedsimultaneously.

Unless otherwise defined, all terms (including technical and scientificterms) used herein have the same meaning as commonly understood by oneof ordinary skill in the art to which this invention belongs. It will befurther understood that terms, such as those defined in commonly useddictionaries, should be interpreted as having a meaning that isconsistent with their meaning in the context of the present applicationand relevant art and should not be interpreted in an idealized or overlyformal sense unless expressly so defined herein. The terminology used inthe description of the invention herein is for the purpose of describingparticular embodiments only and is not intended to be limiting of theinvention. All publications, patent applications, patents and otherreferences mentioned herein are incorporated by reference in theirentirety. In case of a conflict in terminology, the presentspecification is controlling.

Also as used herein, “and/or” refers to and encompasses any and allpossible combinations of one or more of the associated listed items, aswell as the lack of combinations when interpreted in the alternative(“or”).

Unless the context indicates otherwise, it is specifically intended thatthe various features of the invention described herein can be used inany combination. Moreover, the present invention also contemplates thatin some embodiments of the invention, any feature or combination offeatures set forth herein can be excluded or omitted. To illustrate, ifthe specification states that a complex comprises components A, B and C,it is specifically intended that any of A, B or C, or a combinationthereof, can be omitted and disclaimed.

As used herein, the transitional phrase “consisting essentially of” (andgrammatical variants) is to be interpreted as encompassing the recitedmaterials or steps “and those that do not materially affect the basicand novel characteristic(s)” of the claimed invention. See, In re Herz,537 F.2d 549, 551-52, 190 U.S.P.Q. 461, 463 (CCPA 1976) (emphasis in theoriginal); see also MPEP §2111.03. Thus, the term “consistingessentially of” as used herein should not be interpreted as equivalentto “comprising.”

The term “about,” as used herein when referring to a measurable value,such as, for example, an amount or concentration and the like, is meantto encompass variations of ±20%, ±10%, ±5%, ±1%, ±0.5%, or even ±0.1% ofthe specified amount. A range provided herein for a measureable valuemay include any other range and/or individual value therein.

The term “biomass” includes any non-fossilized, i.e., renewable, organicmatter. The various types of biomass may include plant biomass, animalbiomass (any animal by-product, animal waste, etc.) and municipal wastebiomass (residential and light commercial refuse with recyclables suchas metal and glass removed).

The term “plant biomass” or “ligno-cellulosic biomass” includesvirtually any plant-derived organic matter (woody or non-woody)available for energy on a sustainable basis. “Plant-derived” necessarilyincludes both sexually reproductive plant parts involved in theproduction of seed (e.g., flower buds, flowers, fruit, nuts, and seeds)and vegetative parts (e.g., leaves, roots, leaf buds and stems). Plantbiomass can include, but is not limited to, agricultural crop wastes andresidues such as corn stover, wheat straw, rice straw, sugar canebagasse and the like. Plant biomass further includes, but is not limitedto, woody energy crops, wood wastes and residues such as trees, softwoodforest thinnings, barky wastes, sawdust, paper and pulp industry wastestreams, wood fiber, herbal plant material brewing wastes, and the like.Additionally grass crops, such as switchgrass and the like have thepotential to be produced in large-scale amounts and to provide asignificant source of another plant biomass. For urban areas, potentialplant biomass feedstock comprises yard waste (e.g., grass clippings,leaves, tree clippings, brush, etc.) and vegetable processing waste.

The biomass comprises three basic chemical components/fractions, namelyhemicellulose, cellulose, and lignins. The biomass may also includelesser amounts of proteins, extractives, pectins, and ash depending onthe biomass. Specifically, hemicellulose is a polymer (matrixpolysaccharide) comprising the pentose and hexose sugars xylon,glucuronoxylon, arabinoxylon, glucomannon, and xyloglucan. The sugarsare highly substituted with acetic acid, and because of its branchedstructure, hemicellulose is amorphous. Hemicellulose is also easy tocleave via hydrolysis. In contract, cellulose is a linear polymer(polysaccharide) of glucose sugars bonded together by β-glycosidiclinkages to form lengthy linear chains. Hydrogen bonding can occurbetween cellulose chains results in a rigid crystalline structure whichis resistant to cleavage. Lignin is a polymer of phenolic molecules andis hydrophobic. It provides structural integrity to plants, i.e., it isthe glue that maintains the plant intact.

Typical ranges of hemicellulose, cellulose, and lignin in, for example,a plant biomass such as corn stover are:

Component Biomass Dry Weight Cellulose 30-50% Hemicellulose 20-40%Lignin 10-25%

“Ambient temperature” includes the temperature of the surroundings inwhich the process of the invention takes place. Ambient temperature mayinclude, but is not limited to, “room temperature,” and any temperaturewithin the range of 10 to 40° C. (50 to 104° F.).

Individual components of the biomass may include, but are not limitedto, lignin, cellulose, hemicellulose, proteins, pharmaceuticals,nutraceuticals and other materials obtained from the leaves, stems,flowers, buds, roots, tubers, seeds, nuts, fruit and the like of aplant.

“Alcohol” includes, but is not limited to, methanol, ethanol,isopropanol, propanol, isobutanol, butanol, and glycol. A “short chainalcohol” generally includes C₁ to C₄ alcohols.

“Water” includes, but is not limited to, deionized water, spring water,distilled water, mineral water, tap water and well water, and mixturesthereof. “Water soluble” includes a component that can be dissolved inwater or other solvent at ambient temperature. “Water insoluble”includes a component that cannot be dissolved in water or other solventat ambient temperature.

Referring now to FIG. 1, operations for the fractionation and extractionof various biomasses, according to some embodiments of the presentinvention, will be described. A pretreatment step 90 may be conductedoptionally at ambient temperature. The biomass may be subjected to apre-soak step 100 and/or disassembly step 110. The pre-soak step 100 mayinclude contacting with a solvent with or without additives tofacilitate the separation of the individual components. The disassemblystep 110 may include mechanical disassembling of the biomass to providethe biomass in a fluidized or flowable state or condition. After thepretreatment step 90, the biomass may be subjected to high frequencypulses and high shear forces to fractionate 120 or extract via, forexample, the biomass fractionation apparatus and methods described inco-pending U.S. patent application Ser. No. 14/454,833, filed on Aug. 8,2014 (Attorney Docket No. 1237-3) and co-pending U.S. patent applicationSer. No. 14/454,952, filed on Aug. 8, 2014 (Attorney Docket No. 1237-2),the disclosures of which are incorporated by reference in theirentireties. Such fractionation does not denature the one or moreindividual components of the biomass. Such fractionation provides afraction or extracted product that can be separated from thefractionated or extracted biomass. Stated otherwise, the pulsation andshear forces avoid altering the chemical characteristics of theindividual components and does not substantially result in thefragmentation of such components. The fractionated or extracted biomassmay be subjected to separation, namely filtration or screening 125 withor without agitation, followed by a compression force 130, and thenfollowed by additional filtration and/or separation with or withoutagitation 140. The fractions may be used to provide a desired productstream 150. In one embodiment, the amount of hemicellulose and sugars inthe fractionated biomass are monitored such as using a brix meter. Ifsignificant hemicellulose or sugars still are present the steps ofsubjecting to high frequency pulses and shear forces and subjecting tocompressive forces are repeated.

As briefly discussed above, in an initial pretreatment step 90 thebiomass may be pre-soaked and contacted with a solvent such as with analcohol, an aqueous alcohol, water or glycerin or co-solvent or mixturethereof in order to begin the fractionation or extraction of thebiomass. The biomass may swell during this pretreatment step 90. Thebiomass may then be disassembled 110 such as by chopping, cutting,fraying, attrition or crushing prior to contact with the solvent 100. Ina particular embodiment, if the biomass is, for example, fresh plantbiomass or herbal plant material, the material may be contacted withalcohol. If the biomass is dried plant biomass or herbal plan material,it may be contacted with an aqueous alcoholic solution. This aqueousalcoholic extraction may be performed in aqueous alcohol at differentconcentrations. Suitable alcohols may be short chain alcohol, such as,but not limited to, methanol, ethanol, propanol, isopropanol, butanoland isobutanol. In a particular embodiment, the alcohol is ethanol. Thealcohol may be a co-solvent mixture such as a mixture of an alcohol andwater. The aqueous alcoholic solution may comprise from 0-100% (v/v)alcohol. More particularly, the aqueous alcoholic solution may comprisefrom 25-95% (v/v) alcohol. In a particular embodiment, the aqueousalcoholic solution is 25% (v/v) or more alcohol. In another particularembodiment, the aqueous alcohol may be 60% (v/v) alcohol. In anotherembodiment, the aqueous alcoholic solution may be 70% (v/v) alcohol. Inyet another embodiment, the aqueous alcoholic solution may be 86% ormore (v/v) alcohol. In yet other embodiments, the process forfractionating or extracting biomass may comprise contacting the biomasswith glycerin or an aqueous glycerin solution. In yet anotherembodiment, the process for extracting biomass may comprise contactingthe biomass with water. Typically, in other embodiments of theinvention, the ratio of biomass/solids contacted with a solvent/liquidsused may be 1:1 to 1:10 of solids to liquid. During contact with thesolvent (alcohol or water) the fibers of the biomass may swell.

With respect to disassembling the fibers, the fibers are opened up bychopping, cutting, fraying, attrition or crushing the biomass and arethereby provided in a fluidized or flowable form. For example, thebiomass fibers may be processed in a mechanical high consistencyfluidization machine such as a refiner or disk mill. An exemplary diskmill is available from Sprout Waldron, Beloit or Andritz. By utilizing arefiner or disk mill, the biomass and particularly the fibrous materialthereof may be altered without destroying the fibrous nature of thefibrous material so that the high frequency pulses and shear forces ofthe fractionation apparatus are accessible to the fibrous material. Theprocessing may take place for any amount of time necessary as would beunderstood by one of skill in the art as necessary to affect this step.In a particular embodiment, the disassembly process is performed for oneminute or less.

The overall pretreatment step 90 may take place for any period of timethat is sufficient for the fractionation or extraction process and maytake place in any vessel, container or mixer suitable for contacting thebiomass with a solvent and/or disassembling the fibers. In someembodiments, the pretreatment step may be any length of time between,for example, 15 minutes, 30 minutes or one hour, and 72 hours. Inanother embodiment, the pretreatment step may be 15 minutes or less. Thepretreatment step may be one minute or less. In the pretreatment step,the biomass in contact with the solvent may optionally be subjected to acompressive force, which can facilitate absorption of the solvent intothe biomass. The compression in the pretreatment step 90 may take placeaccording to any technique that will be appreciated by one of skill inthe art. In an embodiment of the invention, compression during thepretreatment step may be affected by a screw press.

In another embodiment, the pretreatment may include the addition of anacid to prehydrolyze the biomass to facilitate removal of thehemicellulose. Suitable acids for acidifying the pretreatment solution(solvent) include inorganic acids such as nitric acid, hydrochloric acidand phosphoric acids, and organic acids, such as acetic acid or formicacid. If acidification/hydrolysis is desired, the pH of the solutionwill be about 0.5 to 7.0 and often may be between about 1.0 to 5.0. Asequestering agent or chelating agent such as an aminocarboxylic acid oraminopolyphosphoric acid may also be used.

Additionally a compound to help catalyze delignification may beincluded. In one embodiment, an anthraquinone (AQ) may be utilized.Exemplary anthraquinones and derivatives thereof including1-methylanthrazuinone, 2-methylanthraquinone, 2-ethylanthraquinone,2-methoxyanthraquinone, 2,3-dimethylantraquinone, and2,7-dimethylantraquinone.

In another embodiment an alkaline buffer such as an alkaline metalhydroxide, carbonate phosphate or boron may be included to facilitateseparation of the hemicellulose and lignin individual components.Suitable hydroxides include sodium hydroxide, sodium carbonate, andsodium borate. Mixtures or blends of the hydroxides may be used. If analkaline metal hydroxide is added, the pH may be between about 7.0 to13.0 and often may be between about 8.0 to 11.0.

The pretreatment step 90 may be conducted at ambient temperature,elevated temperature (30° C. to 90° C.) or using steam/vapor (greaterthan 100° C.). It is recognized that the vapor may be of the solvent.

Overall the desire is to provide the fibers in a form wherein thecomponents of the fibers can be readily fractionated using the highshear forces and pulses of the fractionation apparatus. The selection ofthe conditions of the pretreatment step 90 such as solvent choice,temperature, pressure, time, additives, and the like will be dependenton the biomass and the components of that biomass to be fractionated andisolated, and will be within the skill of one in the art without undueexperimentation.

Following disassembly 110, the biomass is in fluid or flowable form maybe subjected to fractionation 120 to fractionate or extract the biomassusing shear forces and pulsation. It will be appreciated that in aparticular embodiment, shear forces and pulsation are used in which thecomponents of the biomass are not denatured or altered, and the chemicalproperties of the individual components are maintained wherein a portionof the fractions or extracts may be separated from the biomass. Thesubjecting of the biomass to shear forces and high frequency pulses maytake place for any amount of time necessary as would be appreciated byone of skill in the art as necessary to affect this step. In aparticular embodiment, this step may takes place for one minute or less.In operation the fluidized biomass is rapidly accelerated from about 4mph to about 120 mph under greater than 1000 pulses per second of energywhile avoiding attrition of the biomass particles. This facilitates theability of the cellular structure of the biomass to release its variousfractions or constituents from the complex and entangled structure ofthe biomass without having the chemical properties and characteristicsof the components being denatured.

The fractionated biomass material may then be subjected to a compressionforce 130 e.g., a crushing or macerating force optionally in thepresence of additional solvent, wherein the compression force removesliquid fraction for collection while discharging a low liquid solidscake primarily being cellulose. The compression force may be appliedaccording to any technique that is appreciated by one of skill in theart. In a particular embodiment, the compression force is affected byscrews of a screw press that macerate the fractionated biomass.

The steps of subjecting to fractionation 120 and subjecting tofractionation can continue until the biomass fraction is substantiallyfree of hemicellulose and sugars. This can be monitored or measured in awide variety of matters including using a brix meter to measure sugarcontent, differential scanning calorimeter (DSC) to measure melttemperatures and differential thermal analysis (DTA) to measure areaunder melt curves.

The fractions or extracts provided according to the present inventionmay be further processed as outlined in FIG. 2. The fractions orextracts provided according to the present invention may be furtherprocessed as outlined in FIG. 2. The screened liquids (e.g., liquidfractions) can be contacted with additional biomass, the biomassdisassembled 210, fractionated 220, screened 240, subjected to acompressive force 230, and the solid fractionated biomass primarilybeing cellulosic and the liquid fractionated product stream separated250. The fractionated biomass is high in cellulose can be used to makepulp and paper.

Once the fractionated biomass is substantially free of hemicellulose andsugars, the biomass is subjected to oxidation at a pH above 7. In oneembodiment, oxidation occurs by contacting the fractionated biomass with0.1 to 1.5 percent hydrogen peroxide. For example, with respect tolignin separation, isolation, and purification, the hydrogen peroxideallows the lignin ether bond to cleave. Specifically, the phenolicgroups in the lignin are ionized and the resulting radical is mainly ofthe phenoxyl radical type. Then hydrogen peroxide is formed throughdismutation of the superoxide anion. The superoxide anion itself is notvery reactive but the decomposition products of hydrogen peroxideinclude the very reactive hydroxyl radical. The hydroxyl radical notonly reacts with the lignin structures but also readily attacks thepolysaccharides with subsequent glycosidic bond cleavage and thecreation of new sites for peeling reactions. Once the perhydoxyl radicalattaches to the lignin (or protein or water insoluble extractive) theseindividual components of the biomass become more polar and watersoluble. Other oxidation agents include alkali metal peroxides such asorganic and inorganic peroxides including sodium peroxide, calciumperoxide, and magnesium peroxide. Moreover this reaction can befacilitated by inclusion of anthraquinone or its derivatives or othercatalysts in the pretreatment step.

After separation, the now water soluble individual components can befurther separated, isolated and/or purified. In one embodiment, thecentrifugation is used to provide a deant. Then, for example,ultrafiltration or diafiltration membranes, available from Millipore,Billerica, Mass., may be used. A first membrane can be used to removeany remaining hemicellulose from the liquid fraction. In one embodiment,the first membrane is a 10K dalton screen. The retentate will comprisethe hemicellulose and the permeate will primarily comprise lignins,proteins, and extractives with a small amount of hemicellulose, sugars,and fiber fragments. The second membrane will isolate the lignin,protein or extractive depending on the membrane as a retentate and anyremaining hemicellulose, sugars, fragments, contaminants (e.g., heavymetals) as the permeate. In one embodiment, the second membrane is an 8Kdalton screen. A further 3K dalton screen can be used to further isolatethe desired component.

In a particular embodiment, the cellulose and/or cellulose pulp providedby the fractionation and/or extraction process of the present inventioncan be used or applied in the preparation of paper and paper products.Examples of paper products include, but are not limited to: paper;paperboard; and card stock. Use of the paper products prepared from thecellulose and/or cellulose pulp provided by the present invention is notparticularly limited. The paper products can be produced with a widevariety of properties, depending on its intended use, which range from,for example: representing value, such as in paper money, bank notes,checks, security, vouchers and tickets; for storing information, such asin books and notebooks, scrapbooks, magazines, newspapers, art, letters;for personal use, such as in diaries, notes to oneself, etc. and scratchpaper; for communication, such as in communication between individualsand/or groups of people; for packaging and containers, such as inpaperboard, kraft board, containerboard, linerboard, beverage and/orfood containers, liquid containers, corrugated boxes, paper bags,envelopes, wrapping tissue, Charta emporetica and wallpaper; forcleaning, such as in toilet paper, handkerchiefs, paper towels, facialtissue and cat litter; for construction, such as in papier-mâché,origami, paper planes, quilling, paper honeycomb, used as a corematerial in composite materials, paper engineering, construction paperand paper clothing; and other uses, such as in emery paper, sandpaper,blotting paper, litmus paper, universal indicator paper, paperchromatography, electrical insulation paper (see also dielectric andpermittivity) and filter paper.

The method by which the cellulose and/or cellulose pulp provided by thepresent invention is used in the production of paper and paper productsis not particularly limited, and any method that would be appreciated byone of skill in the art may be used in the production of paper and paperproducts using the cellulose and/or cellulose pulp provided by thepresent invention. For example, the cellulose pulp provided according tothe present invention can be fed to a paper machine where it is formedas a paper web and the water is removed from it by pressing and drying.The cellulose pulp provided by the present invention may also bebleached to make the pulp whiter. Typical chemicals and processes usedin the bleaching of pulp include: chlorine; sodium hypochlorite;extraction with sodium hydroxide; oxygen; alkaline hydrogen peroxide;ozones; chelation to remove metals; enzyme treatment; peroxy acids; andsodium dithionite. Typical chelation agents include, but are not limitedto, EDTA and DTPA. Although not particularly limited by the method ofbleaching of the cellulose and/or cellulose pulp provided by the presentinvention, elemental chlorine free (ECF) and/or total chlorine free(TCF) methods of bleaching provide more environmentally friendly methodsof bleaching. TCF bleaching, for example, prevents the formation oftoxic chemicals such as dioxins. An example of a TCF sequence for thebleaching of pulp is wherein the pulp would be treated with oxygen, thenozone, washed with sodium hydroxide then treated in sequence withalkaline peroxide and sodium dithionite.

In other embodiments, the cellulose and/or cellulose pulp providedaccording to the present invention can be used or applied in thepreparation and/or manufacture of paper coatings. Cellulose andcellulose derivatives have been used to coat papers to enhance physicalcharacteristics, for example, but not limited to, appearance, e.g.,glossiness and finish, strength, rigidity and water resistance. Themanner in which the paper coatings prepared from the cellulose and/orcellulose pulp provided according to the present invention is notlimited and the method used may be any that would be appreciated by oneof skill in the art.

In yet other embodiments, the cellulose and/or cellulose pulp providedaccording to the present invention can be used in the preparation offibers. Examples of fibers include, but are not limited to, regeneratedcellulose fibers, for example, cellophane and rayon.

In yet other embodiments, the cellulose and/or cellulose pulp providedaccording to the present invention can be used in consumables. The typeof consumable is not particularly limited, and applications can include,but are not limited to: microcrystalline cellulose or powdered celluloseused as inactive fillers in drug tablets; thickeners and/or stabilizersPowdered cellulose may also be used to improve characteristics ofprocessed foods or foodstuffs, for example, to prevent caking and/orclumping of the processed food or foodstuffs within a container.

In yet other embodiments, the cellulose and/or cellulose pulp providedaccording to the present invention can be used in scientificapplications. Cellulose is commonly used in the laboratory as thestationary phase for chromatography, in particular, thin layerchromatography. Liquid and gel filtration typically use productsprepared from cellulose, either alone or in combination with otherfiltration media, for example, diatomaceous earth.

In yet other embodiments, the cellulose and/or cellulose pulp providedaccording to the present invention can be used in construction andbuilding materials. Cellulose insulation made from recycled paper isbecoming popular as an environmentally preferable material for buildinginsulation. It can be treated with boric acid as a fire retardant.Moreover, hydrogen bonding of cellulose in water can produce asprayable, moldable material as an alternative to the use of plasticsand resins. The recyclable material can be made water and/orflame-resistant or fire retardant, and can provide sufficient strengthfor use as a building material.

In another embodiment, the cellulose can be treated with celluloseenzymes to hydrolyze the crystalline cellulose to glucose followed byfermentation of the glucose with yeast or suitable microorganism toprovide biofuel and/or bio feedstock. It is recognized that thehemicellulose and/or sugars previously separated from the fractionatedbiomass may be added back to be co-fermented with the cellulose.

In another particular embodiment, fractionation or extraction accordingto the invention provides hemicelluloses and sugars. Sugars and/orhemicelluloses provided by the process according to the invention mayfurther be used in the preparation of biofuels such as, but not limitedto, ethanol or the preparation of polymers/plastics. One such embodimentis the fermentation of the provided fractions to produce the ethanol. Inanother embodiment, the polymer is polylactic acid (PLA). In anotherembodiment the lignin may be further separated and emulsified forfurther processing. Because the lignin has not been subjected to hightemperatures, its functional groups have not chemically reacted and theisolated lignin may be more reactive.

In another embodiment of the invention, the fraction or extract isolatedand used is lignin. Examples of the applications and uses of ligninprovided by the present invention include, but are not limited to, forexample: cement and concrete; animal feed pellets; animal feed molassesadditives; road binder/dust control; pesticides; oil well drilling muds;adhesives; resins and binders; wallboard; dispersants; emulsifiers andwetting agents; agglomerants; chelants; leather treatment;anti-bacterial activity; lead acid batteries; oil recovery; watertreatment; industrial cleaners; emulsion stabilizers; carbon black; inksand azo pigments; dyestuffs; micronutrients; fertilizers; refractoriesand ceramic brick additives; ore processing; and kitty litter. Inanother embodiment of the invention, the fraction or extract used ispulp, cellulose and/or cellulose pulp. Examples of the applications anduses and applications of cellulose and/or cellulose pulp provided by thepresent invention include, but are not limited to, for example: paperand paper products; paper coatings; fibers; consumables; science;biofuels; building materials; insulation adhesives; and binders.

In some embodiments, the lignin provided according to the presentinvention may comprise derivatives of lignin or lignin derivatives, forexample, lignosulfonates or lignin amine. In a further embodiment, thelignin provided by the present invention is used as a binder. Lignin orlignin derivatives can be used as an adhesive, serving as a bindingagent in pellets or compressed materials. Lignin or lignin derivativescan be used in dust control, for example, on unpaved roads to reduceenvironmental concerns from airborne dust particles and stabilize theroad surface. The ability of lignin to act as a binder makes ligninuseful as a component in, for example: biodegradable plastic; coalbriquettes; plywood and particle board; ceramics; animal feed pellets;carbon black; fiberglass insulation; fertilizers and herbicides;linoleum paste; dust suppressants; and soil stabilizers.

In other embodiments, the lignin provided by the present invention isused as a dispersant. Lignin or lignin derivatives can prevent theclumping and settling of undissolved particles in suspensions. Lignin orlignin derivatives can prevent particles in suspension from beingattracted to other particles and can reduce the amount of water neededto use a product comprising said particles in suspension. The ability oflignin or lignin derivatives to act as a dispersant make lignin usefulas a component in, for example: cement mixes; leather tanning; clay andceramics; concrete admixtures; dyes and pigments; oil drilling muds; andpesticides and insecticides.

In still other embodiments, the lignin provided according to the presentinvention is used as an emulsifier. Lignin or lignin derivatives maystabilize emulsions of immiscible liquids, for example, oil and water,making them highly resistant to separating. The ability of lignin,lignosulfates and lignin amine to act as an emulsifier makes lignin orlignin derivatives a useful component in, for example: asphaltemulsions; pesticides; pigment and dyes; and wax emulsions.

In yet other embodiments, lignin provided according to the presentinvention is used as a sequestrant. Lignin or lignin derivatives caninteract with metal ions, preventing them from reacting with othercompounds and becoming insoluble. Metal ions sequestered with lignin orlignin derivatives stay dissolved in solution, rendering them availableto plants and preventing scaly deposits in water systems. The ability oflignin and lignin derivatives to act as a sequestrant makes lignin auseful component in, for example: micronutrient systems; cleaningcompounds; and water treatments for boilers and cooling systems.

In a particular embodiment, lignin provided by the present invention canbe used in concrete. Lignin or lignin derivatives can aid in, forexample: high performance concrete strength; concrete grinding; reducingdamage caused by moisture and acid rain; and retarding cementcomposition setting. Specifically, lignosulfonates can contribute higheradsorption properties and zeta potential to cement particles and providebetter dispersion characteristics to the cement matrix. Lignins can alsoimprove the compressive strength of cement pastes.

In another embodiment, lignin provided by the present invention can beused as an antioxidant. Lignin can act as a free radical scavenger, andprovide thermal protection to, for example, styrene polymers, butadienepolymers, rubber polymers, rubber, polypropylene and polycaprolactam.The natural antioxidant properties of lignin make it useful in cosmeticand topical formulations, and lignosulfonates have been used in cosmeticcompositions, such as makeup for decorative use and/or correction onskin.

In yet another embodiment, lignin provided by the present invention canbe used in asphalt. Examples of uses include crack filling compositionsfor asphalt, enhancing water stability of asphalt, emulsifying agentsfor asphalt and fluidity modifiers that decrease production costs ofasphalts.

In another particular embodiment, lignin provided by the presentinvention may be applied to and/or used in or with carbon or graphitefibers, carbon fiber reinforced polymers and carbon nanotubes.

In yet another particular embodiment, lignin provided by the presentinvention may be applied and used in the production of fiberboards,particleboards, wood fiber insulation boards, strawboards, orientedstrand boards and the like as part of a binder composition. For example,a lignin may be added to a resin to provide a binder with reasonable wetstrength. Lignin based modifiers, wherein lignin or lignosulfonate canbe added to formaldehyde based binder systems, for example, phenolformaldehyde, urea formaldehyde, melamine formaldehyde, resorcinolformaldehyde and/or tannin formaldehyde resins. The resulting boardbinder may then be used for panel boards, for example, in plywoods, hardboards, fiberboards or particle boards.

In another embodiment, lignin provided by the present invention may beapplied and used in foams, plastics and/or polymers. For example,polyurethanes comprising lignins can have improved flame resistanceand/or fire retardance. Epoxy resins can comprise a curing agent thatcomprises a lignin and/or a lignin derivative, such as a lignin-derivedacetic anhydride. Lignins, for example S-free lignin, can be used inepoxy resins for fabricating printed circuit boards, or in products,such as automotive brakes. Lignins may be added to polymers, forexample, polyphenylene oxide-based polymers, to enhance modulus ofelasticity, tensile strength and elongation at break values of thepolymer. Lignin can also act as a water absorption inhibitor and/or as afluidization agent to facilitate polymer, for example, polyamide,processing, such as by injection molding, blow molding, extrusion orblow extrusion, to fabricate articles when mixed in solid or melt form.Lignins, for example, alkali lignin poly(propylene carbonate), can alsobe used to improve the thermal stability and mechanical properties ofpolymers.

In yet another embodiment, lignin provided by the present invention maybe applied and used in dust control. For example, lignin and glycerin inwater, can be applied to areas in which dust is a problem, such as, forexample, in coal mines, transportation of coal, railways, roads, stockyards and the like. Lignin, for example, particular calcium ligninsulfonate powders, have been shown to stabilize contamination followinga nuclear accident. Dust movement can also be controlled on a roadsurface by spraying with an emulsion comprising asphalt, lignosulfonateand water.

In another particular embodiment, lignin provided by the presentinvention may be applied and used in papers as a sizing agent, toenhance paper tensile strength, and/or as a packaging laminate.

In yet another embodiment, lignin provided by the present invention maybe applied and used to provide chemicals through depolymerization oflignin. Depolymeriziation of lignin can provide, for example, phenols,cresols, catechols, resorcinols, quinolines, vanillin, guaiacols and thelike.

In yet another embodiment, lignin provided by the present invention maybe applied and used in batteries and to enhance the performance ofenergy storage devices. For example, graphite powder in batteriescomprising a thin layer of lignin can be used to prevent the graphitepowder from decreasing H overvoltage, while not affecting the conditionof the graphite powder. Lignin can also be used to protect negativeplates of batteries from the formation of a passivating lead sulfatelayer thereon.

In yet another particular embodiment, lignin provided by the presentinvention may be applied and used as a fuel additive, or can becatalytically converted to gasoline/diesel by a combination ofpyrolysis, thermal cracking, hydrocracking, catalytic cracking orhydrotreatment. Lignin may further be used in catalytic hydrothermalgasification to provide fuel gas. Lignin may also be used to woodpellets to produce better quality pellets with higher fuel value, or inartificial fire logs to provide improved flame properties.

In another embodiment, lignin provided by the present invention may beapplied and used as an additive to improve the characteristics oflubricants. For example, lignosulfonates can be used as a thickeningagent for lubricating greases. Greases can comprise lignin compositionsto provide improved corrosion protection properties of the grease.Additionally, greases comprising lignin, for example, hydrolytic lignin,can provide greater wear resistance to devices using the same. Greasescomprising lignin, such as lignosulfonate, can improve the antifrictionproperties of the grease, and provide longer lubrication life for thegrease.

In yet another particular embodiment, lignin provided by the presentinvention may be applied and used in the production of latex and/orrubber. For example, lignin can be added to latex and/or rubber andfunction as a filler, pigment, modifier, extender or reinforcement forthe same. Lignin added to latex can increase oil resistance and/ortensile strength of rubber latex films. Rubbers reinforced with lignincan exhibit improved ozone resistance compared to rubbers without ligninadded. The method by which the lignin provided by the present inventionis incorporated into latex and/or rubber is not particularly limited,and may be carried out by in any manner that will be appreciated by oneof skill in the art.

In another embodiment, the isolated proteins may be further isolated andhydrolyzed to single amino acids, peptides, and/or polypeptides.Isolated protein may be used as a food supplement for humans andanimals. The protein content can be measured using Kjeldehl analysis.

The following example is provided to illustrate the present invention,and should not be construed as limiting thereof.

EXAMPLE Example 1 Wheat Grass

10 Kg of dried wheat grass (straw) is chopped to a stalk length of ¾ to2 inches. The straw was briefly rinsed with cold clean water to removesand and dirt. The wheat straw is then subjected to water or steaminjection into a disk mill for a few seconds to mechanically disassemblethe cellulosic structure. The fluidized wheat grass is then subjected tohigh shear forces for 1.5 to 3 seconds with pulses of 1824 to 912 timeswithout denaturing the components of the wheat straw. The combinedmixture is subjected to compressive forces to separate the stream intoliquid and a 20-60% cellulosic solids fractions. The liquid fractioncontaining hemicellulose is retained.

The solid fraction is pretreated with NaOH sufficient to raise the pH ofthe cellulosic water slurry from about 4-7 to 10-12. This basic mixtureis allowed to age from a few seconds to 1 hour and again processedthrough the system starting at the disk mill which is subjected to wateror steam injection in the mill for a few seconds to mechanicallydisassemble the cellulosic structure. The fluidized wheat grass is thensubjected to high shear forces for 1.5 to 3 seconds with pulses of 1824to 912 times without denaturing the components of the wheat straw. Thecombined mixture is subjected to compressive forces to separate thestream into liquid and a 20-60% cellulosic solids fractions. The liquidfraction containing hemicellulose is added to the first and secondfraction and undergoes further processing.

The solid fraction is treated with an oxidation agenti hydrogenperoxide, sufficient to raise the pH of the cellulosic water slurry fromabout 10-12 to 8-10. This basic mixture is allowed to age from a fewseconds to 1 hour and again processed through the system starting at thedisk mill which is subjected to water or steam injection in the mill fora few seconds to mechanically disassemble the cellulosic structure. Thefluidized wheat grass is then again subjected to high shear forces for1.5 to 3 seconds with pulses of 1824 to 912 times without denaturing thecomponents of the wheat straw. The combined mixture is screened andsubjected to compressive forces to separate the stream into liquid and a20-60% cellulosic solids fractions. The liquid fraction containinglignin is retained. The solid fraction is then treated again to raisethe pH and the liquid fraction containing hemicellulose is added to thefirst and second fraction and undergoes further processing. The solidfraction is then treated with an oxidation agent and rerun through thefractionation unit. The liquid fraction containing lignin is added tothe first liquid lignin fraction and further separated using a membrane.

Although selected embodiments of the present invention have beendisclosed for illustrative purposes, those skilled in the art willappreciate that various modifications, additions and substitutions arepossible, without departing from the scope and spirit of the inventionas disclosed in the accompanying claims.

That which is claimed is:
 1. A process for providing water insolublecomponents of a biomass in water soluble form and a biomasssubstantially devoid of hemicellulose, sugar and the water insolublecomponents, the process comprising: a) pretreating the biomass with afirst basic solution; b) subjecting the pretreated biomass to highfrequency pulses and shear forces without denaturing the individualcomponents of the biomass; c) subjecting the biomass to compressiveforce to separate a first liquid fraction from a first fractionatedbiomass; d) subjecting the first fractionated biomass to the same highfrequency pulses and shear forces of step b); e) subjecting the firstfractionated biomass to compressive forces to separate a second liquidfraction from a second fractionated biomass wherein the secondfractionated biomass is substantially devoid of hemicelluloses andsugars; f) subjecting the second fractionated biomass substantiallydevoid of hemicelluloses and sugars to oxidation at a pH above 7; and g)subjecting the second fractionated biomass to compressive force toseparate one or more water insoluble components of the biomass in watersoluble form from a second fractionated biomass substantially devoid ofhemicellulose, sugar and the water insoluble components of the biomass.2. The process of claim 1, further comprising after step e) contactingthe second fractionated biomass substantially devoid of hemicellulosesand sugars with a second basic solution and subjecting the secondfractionated biomass to compressive force to separate at least one firstwater insoluble component of a biomass in water soluble form from thesecond fractionated biomass substantially devoid of hemicelluloses andsugars.
 3. The process of claim 2, wherein the first and second basicsolutions comprise sodium hydroxide.
 4. The process of claim 1 whereinthe steps are conducted at ambient temperature to about 60° C.
 5. Theprocess of claim 1 wherein step f) of subjecting the second fractionatedbiomass substantially devoid of hemicelluloses and sugars to oxidationincluded contacting the second fractionated biomass substantially devoidof hemicelluloses and sugars with a hydrogen peroxide solution.
 6. Theprocess of claim 1, wherein the water insoluble component of a biomassin water soluble form is purified by contacting with a membrane.
 7. Awater insoluble component of a biomass in water soluble form provided bythe method claim
 1. 8. A process for providing water insolublecomponents of a biomass in water soluble form and a biomasssubstantially devoid of hemicellulose, sugar and the water insolublecomponents, the process comprising: a) pretreating the biomass with afirst basic solution; b) subjecting the pretreated biomass to highfrequency pulses and shear forces without denaturing the individualcomponents of the biomass; c) subjecting the biomass to compressiveforce to separate a first liquid fraction from a first fractionatedbiomass; d) monitoring the amount of hemicellulose in the firstfractionated biomass to determine if first fractionated biomasssubstantially devoid of hemicellulose and sugar, e) subjecting the firstfractionated biomass, if not devoid of hemicellulose and sugar to thesame high frequency pulses and shear forces of step b); f) subjectingthe first fractionated biomass to compressive forces to separate asecond liquid fraction from a second fractionated biomass wherein thesecond fractionated biomass is substantially devoid of hemicellulosesand sugars; g) subjecting the second fractionated biomass substantiallydevoid of hemicellulose and sugars to oxidation at a pH above
 7. h)subjecting the second fractionated biomass to compressive force toseparate one or more water insoluble components of the biomass in watersoluble form from a second fractionated biomass substantially devoid ofhemicellulose, sugar and the water insoluble components of the biomass.9. The process according to claim 1, wherein the organic solvent isselected from the group consisting of methanol, ethanol, propanol,butanol, and glycol.
 10. The process according to claim 1, wherein thesolvent is any one selected from a group consisting of a short chainalcohol, glycerin and water, or a co-solvent mixture of any combinationthereof.
 11. A water insoluble component of a biomass in water solubleform selected from the group consisting of lignins, proteins andextractives, wherein the water soluble form selected from the groupconsisting of lignins, proteins and extractives is soluble in water atabout a pH of 5 to 12 at ambient temperature.